Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_assertion description "[EWS-FLI1 fusion type, p53 mutation, and homozygous deletion of p16/p14ARF have each been shown to be prognostically significant in Ewing sarcoma (ES).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_assertion evidence source_evidence_literature NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_assertion SIO_000772 15659501 NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_assertion wasDerivedFrom befree-2016 NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_assertion wasGeneratedBy ECO_0000203 NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.
- befree-2016 importedOn "2016-02-19" NP476927.RAsXWzItIHfEDV3O4ofNxbqADe_asos00-2z7aoomGWXo130_provenance.